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UnknownNon-Linear Association of Dietary Polyamines with the Risk of Incident Dementia: Results from Population-Based Cohort of the UK Biobank.
Not available
S-EPMC11357304 | biostudies-literature
UnknownIntegrating Genetic Mapping and BSR-Seq Analysis to Identify Candidate Genes Controlling Fruitfulness in <i>Camellia sinensis</i>.
Not available
S-EPMC12526348 | biostudies-literature
UnknownSRSF1 promotes the inclusion of exon 3 of SRA1 and the invasion of hepatocellular carcinoma cells by interacting with exon 3 of SRA1pre-mRNA.
Not available
S-EPMC8134443 | biostudies-literature
UnknownTruncated SCRIB isoform promotes breast cancer metastasis through HNRNP A1 mediated exon 16 skipping.
Not available
S-EPMC10618471 | biostudies-literature
UnknownSilencing of the lncRNA H19 enhances sensitivity to X-ray and carbon-ions through the miR-130a-3p /WNK3 signaling axis in NSCLC cells.
Not available
S-EPMC8642868 | biostudies-literature
ProteomicsDistinct amyloid fibril structures formed by ALS-causing SOD1 mutants G93A and D101N
We expressed and purified recombinant full-length wild-type human SOD1 and its G93A and D101N variants in Expi293F cells where the initiating Met was removed and the N-terminus at Ala1 was acetylated, and identified N-terminal acetylation of the mammalian cell–purified G93A , D101N , and wild-type S...
ORGANISM(S): Homo sapiens (Human) 
2025-10-20 | PXD066116 | Pride
Amyotrophic lateral sclerosis (als)  sod1 mutants  amyloid fibrils  cryo-em structure  toxicity. 
UnknownSTARD4 suppresses tumorigenesis and attenuates enzalutamide resistance via lipid metabolic reprogramming and AR stabilization in prostate cancer.
Not available
S-EPMC12699821 | biostudies-literature
GenomicsDAC for Dave Lab, Duke University
Data Access Committee EGAC00001000538
EGAC00001000538 | EGA
Genomicsena-DATASET-DAVELAB-22-03-2017-21:30:50:663-38 - samples
Whole exome sequencing of hepatosplenic T cell lymphoma (HSTL) tumors, paired normals, and cell lines, including (1) 68 exome capture, paired-end Illumina Hiseq sequencing, BAM files from HSTL tumor samples, (2) 20 exome capture, paired-end Illumina Hiseq sequencing, BAM files from HSTL paired norma...
EGAD00001003246 | EGA
GenomicsGenetic Basis of Hepatosplenic T Cell Lymphoma (HSTL)
Hepatosplenic T cell lymphoma (HSTL) is a rare and lethal lymphoma; the genetic drivers of this disease are unknown.  Through whole exome sequencing of 68 HSTLs, we define recurrently mutated driver genes and copy number alterations in the disease. Chromatin modifying genes including SETD2, INO80 an...
EGAS00001002182 | EGA
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